C8orf37

chromosome 8 open reading frame 37
OMIM: 614477
PanelMode of inheritanceDetails
4 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 3.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
CONE-ROD DYSTROPHY 16 614500
R-numbers: R21, R412
Signed-off version 2.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
CONE-ROD DYSTROPHY 16
Component of the following Super Panels:
  • - Paediatric disorders
  • - Rare multisystem ciliopathy Super panel
Signed-off version 2.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Bardet-Biedl syndrome 21, OMIM:617406, MONDO:0044308, Cone-rod dystrophy 16, OMIM:614500, MONDO:0013786, Retinitis pigmentosa 64, OMIM:614500, MONDO:0019200
R-numbers: R32
Signed-off version 3.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Bardet-Biedl syndrome 21, OMIM:617406, MONDO:0044308, Cone-rod dystrophy 16, OMIM:614500, MONDO:0013786, Retinitis pigmentosa 64, OMIM:614500, MONDO:0019200